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An efficient hybrid feature selection method to identify potential biomarkers in common chronic lung inflammatory diseases

机译:一种有效的杂交特征选择方法,以识别常见慢性肺炎疾病中潜在的生物标志物

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Asthma, chronic obstructive pulmonary disease (COPD), and idiopathic pulmonary fibrosis (IPF) are three serious lung inflammatory diseases. The understanding of the pathogenesis mechanism and the identification of potential prognostic biomarkers of these diseases can provide the patients with more efficient treatments. In this study, an efficient hybrid feature selection method was introduced in order to extract informative genes. We implemented an ontology-based ranking approach on differentially expressed genes following a wrapper method. The examination of the different gene ontologies and their combinations motivated us to propose a biological functional-based method to improve the performance of further wrapper methods. The results identified: TOM1L1, SRSF1, and GIT2 in asthma; CHCHD4, PAIP2, CRLF3, UBQLN4, TRAK1, PRELID1, VAMP4, CCM2, and APBB1IP in COPD; and TUFT1, GAB2, B4GALNT1, TNFRSF17, PRDM8, and SETDB2 in IPF as the potential biomarkers. The proposed method can be used to identify hub genes in other high-throughput datasets.
机译:哮喘,慢性阻塞性肺病(COPD)和特发性肺纤维化(IPF)是三种严重的肺炎疾病。理解致病机制和这些疾病的潜在预后生物标志物的鉴定可以为患者提供更有效的治疗方法。在该研究中,引入了一种有效的混合特征选择方法,以提取信息基因。在包装方法之后,我们在差异表达基因上实现了基于本体的排名方法。对不同基因本体的检查及其组合的激励我们提出了一种基于生物功能的方法,以提高进一步包装方法的性能。结果确定:哮喘中的Tom1L1,SRSF1和Git2; CHCHD4,PAIP2,CRLF3,UBQLN4,TRAK1,PRELID1,VAMP4,CCM2和APBB1IP在COPD中; IPF中的TNFRSF17,PRDM8和SETDB2作为潜在的生物标志物。该方法可用于识别其他高通量数据集中的集线器基因。

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